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Transducer Cover
Vitrolife Sweden AB · Model 14201 · UDI-DI 17350025911646
HEM
Prescription
1
510(k) clearances
1
Adverse events
1
Recalls
1
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-05-12 | Digisonics, Inc | Data/measurements from a OB report sent from ultrasound systems populated the wrong OB-View report |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
